Thiosinaminum
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Thiosinaminum
- Generic name
- THIOSINAMINUM
- Manufacturer
- Hahnemann Laboratories, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f1f61f7e-bb40-4ee8-e053-2a95a90a08bd
- SPL ID
- f1f61f7e-bb41-4ee8-e053-2a95a90a08bd
- Version
- 1
- Effective date
- 2023-01-10
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:23:20
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Thiosinaminum | openfda.brand_name | |
| generic name | THIOSINAMINUM | openfda.generic_name | |
| manufacturer name | Hahnemann Laboratories, INC. | openfda.manufacturer_name | |
| ndc | package | 37662-2309-1 | openfda.package_ndc |
| ndc | package | 37662-2308-1 | openfda.package_ndc |
| ndc | package | 37662-2309-3 | openfda.package_ndc |
| ndc | package | 37662-2306-2 | openfda.package_ndc |
| ndc | package | 37662-2311-3 | openfda.package_ndc |
| ndc | package | 37662-2310-3 | openfda.package_ndc |
| ndc | package | 37662-2312-1 | openfda.package_ndc |
| ndc | package | 37662-2306-1 | openfda.package_ndc |
| ndc | package | 37662-2307-2 | openfda.package_ndc |
| ndc | package | 37662-2305-2 | openfda.package_ndc |
| ndc | package | 37662-2308-4 | openfda.package_ndc |
| ndc | package | 37662-2308-2 | openfda.package_ndc |
| ndc | package | 37662-2307-1 | openfda.package_ndc |
| ndc | package | 37662-2309-4 | openfda.package_ndc |
| ndc | package | 37662-2310-1 | openfda.package_ndc |
| ndc | package | 37662-2310-4 | openfda.package_ndc |
| ndc | package | 37662-2311-4 | openfda.package_ndc |
| ndc | package | 37662-2305-3 | openfda.package_ndc |
| ndc | package | 37662-2305-1 | openfda.package_ndc |
| ndc | package | 37662-2309-2 | openfda.package_ndc |
| ndc | package | 37662-2306-3 | openfda.package_ndc |
| ndc | package | 37662-2311-2 | openfda.package_ndc |
| ndc | package | 37662-2311-1 | openfda.package_ndc |
| ndc | package | 37662-2310-2 | openfda.package_ndc |
| ndc | package | 37662-2308-3 | openfda.package_ndc |
| ndc | package | 37662-2307-3 | openfda.package_ndc |
| ndc | package | 37662-2307-4 | openfda.package_ndc |
| ndc | product | 37662-2306 | openfda.product_ndc |
| ndc | product | 37662-2307 | openfda.product_ndc |
| ndc | product | 37662-2305 | openfda.product_ndc |
| ndc | product | 37662-2308 | openfda.product_ndc |
| ndc | product | 37662-2310 | openfda.product_ndc |
| ndc | product | 37662-2312 | openfda.product_ndc |
| ndc | product | 37662-2311 | openfda.product_ndc |
| ndc | product | 37662-2309 | openfda.product_ndc |
| ndc11 | package | 37662230701 | derived:openfda.package_ndc |
| ndc11 | package | 37662230904 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.